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作 者:何杨[1] 金坚[1] 赵益明[1] 沈文红[1] 阮长耿[1]
机构地区:[1]苏州医学院血栓与止血研究室.江苏省血液研究所,苏州215007
出 处:《标记免疫分析与临床》1998年第1期38-41,共4页Labeled Immunoassays and Clinical Medicine
基 金:国家自然科学基金;中国核工业总公司科研基金资助
摘 要:从利凡诺去白蛋白人血浆中提纯了蛋白C抑制物,抗血清由免疫家兔产生,“’互一蛋白C抑制物用Iodogen法制备,采用平衡法建立RIA,数据用四参数logistic数据处理程序处理。方法的批内和批间CV分别为2.73%和8.62%,平均回收率为101.89%,可测范围为4.8~1024pg/L,ED50为19.34μg/L。40名健康男、女性血浆蛋白C抑制物含量为4.69土1.8mg/L(),本方法可为血栓、栓塞性疾病的诊疗和蛋白C系统的基础及临床研究提供一种有效的手段。A radioimmunoassay of protein C inhibitor(PCI) was established. PCI was purified from albumin free human plasma by rivanol precipitation, and the antiserum was obtained byimmunizing the rabbits. The 125I - PCI was prepared by the lodogen method. The data wereprocessed by the four - parameter logistic RIA program. Methodological study found that the intra- and inter - C. V. was 2. 73 % and 8. 62 %, respectively, and the recovery rate was 101. 89 %.The range of measurement was 4. 8 ~ 1024μg/L, and ED5o was 19. 34 μg/L. No cross - reactivitywas found with thrombin, antithrombin Ⅲ, protein C, protein S and thrombomodulin. Humanplasma samples were assayed and the plasma PCI level of 40 healthy volunteers was 4. 69 ±1.sing/L(x ±2s ). This new method can be used as an effective tool especially for diagnosis ofthrombosis and the basic or clinical study of protein C system.
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